L. Perrigo recalls 180mg Fexofenadine tablets with impurities that could pose health risks. Check NDC 68391-847-47 and lot numbers for affected products.
Failed Impurities/Degradation Specifications
L. Perrigo is recalling non-drowsy allergy relief tablets that may contain impurities. This could pose health risks to users, especially if the tablets are taken without proper quality control.
The tablets may contain impurities that could cause health issues if taken. This is due to failed impurities and degradation specifications during manufacturing.
People who purchased the recalled 180mg Fexofenadine tablets from BJ's Wholesale Club are affected. Those with allergies or sensitive health conditions may be at higher risk.
Check for NDC 68391-847-47 on the product label. The lot numbers include 2DV1863, 2HV2698, 2GV1583, 2HV2697, and expiration dates up to 12/23.
Look for NDC 68391-847-47 and lot numbers 2DV1863, 2HV2698, 2GV1583, 2HV2697 on the product label.
The product failed impurities and degradation specifications, which could pose health risks.
Check for NDC 68391-847-47 and lot numbers 2DV1863, 2HV2698, 2GV1583, 2HV2697 on the product label.
The recall record does not specify a remedy, so contact L. Perrigo Company for guidance.
We’ve drafted a message you can send L. Perrigo Company to request your refund or repair — edit it as you like.
Subject: Recall D-0901-2023 — L. Perrigo Company L. Perrigo Company Hello, I own a L. Perrigo Company that is covered by recall D-0901-2023 from L. Perrigo Company. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
